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loading...| Preferred Name |
Obesity due to leptin receptor gene deficiency |
| ID |
http://www.orpha.net/ORDO/Orphanet_179494 |
| definition |
A rare, genetic, non-syndromic, obesity disease characterized by severe, early-onset obesity, associated with major hyperphagia and endocrine abnormalities, resulting from leptin receptor deficiency. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=179494 |
| hasDbXref |
ICD-11:5B81.Y OMIM:614963 ICD-10:E66.8 |
| label |
Obesity due to leptin receptor gene deficiency |
| notation |
Etiological subtype ORPHA:179494 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_179494 |
| prefLabel |
Obesity due to leptin receptor gene deficiency |
| treeView | |
| subClassOf |